Life Science Job at Alimentiv | Apply Now
Looking for a life science job in clinical research and imaging? This opportunity at Alimentiv offers a dynamic role in imaging research and development, where you’ll collaborate with global clinical teams, contribute to central image management solutions, and gain hands-on experience in clinical trials. If you’re passionate about imaging research and want to explore Alimentiv careers or even transition into a remote job environment, this role could be the perfect fit.
- Job Position: Imaging Research and Development Associate (1-year contract)
- Location: Remote
About the Company
Alimentiv is a global organization specializing in clinical research and imaging solutions, supporting clinical trials through advanced Central Image Management Solution (CIMS) services. Known for innovation in imaging research, Alimentiv careers offer professionals opportunities to work on cutting-edge clinical projects with global impact.
Job Description
The Imaging Research and Development Associate will assist with providing the Clinical Project Management, Data Management and Medical Leadership teams with medical, scientific, and operational advice/support for Central Image Management Solution (CIMS) clinical trials. Act as a point of contact assisting in issues/matters related to central reading with internal and external project teams. Collaborate with internal and external stakeholders on document development, central reader training and quality monitoring, and assist in analyzing image services and product offerings for CIMS clinical trials. Support the department and company in achieving objectives and strategic goals.
Qualifications
Education
- Bachelor’s Degree (preferred: Life Sciences, Clinical Research, or Medical Imaging)
Skills
- Strong analytical and problem-solving skills
- High learning agility
- Ability to work effectively in ambiguous and dynamic environments
Key Responsibilities
Trials Management Support
- Act as a point of contact for internal and external project teams on medical/scientific matters related to central reading
- Escalate issues to Medical Leadership, Scientific Advisors/Collaborators, and Central Readers when required
- Participate in internal and sponsor meetings
- Analyze and implement project-specific imaging requirements (quality control processes, central reading paradigms, etc.)
- Lead development of Image Review Charters and Central Reader Variability Monitoring documentation
- Contribute to creation of project-specific documents (Work Instructions, process flows, manuals)
- Prepare and maintain site training materials related to imaging standards and scoring indices
Central Reading Processes Support
- Develop and review central reader training materials
- Participate in quality monitoring activities and trainings
- Review statistical data outputs and raw data to identify trends/issues
- Support development of mitigation strategies and process improvements
- Act as a contact point for central reading issues and improvements
Process/Product Design and Improvements
- Collaborate with cross-functional teams on new imaging technologies and process improvements
- Support development and maintenance of SOPs and Work Instructions
- Participate in imaging modality-specific working groups and committees
Research and Development
- Collaborate with Medical Leadership and Scientific Advisors on imaging standards and study design
- Contribute to improvements in imaging processes (central reading, quality control, monitoring)
- Support continuous improvement through knowledge sharing, training, and education
